Package 15014-910-10

Brand: methocarbamol

Generic: methocarbamol
NDC Package

Package Facts

Identity

Package NDC 15014-910-10
Digits Only 1501491010
Product NDC 15014-910
Description

100 TABLET in 1 BOTTLE (15014-910-10)

Marketing

Marketing Status
Marketed Since 2025-05-22
Brand methocarbamol
Generic methocarbamol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "35c044a6-90c1-55f8-e063-6294a90aad48", "openfda": {"nui": ["N0000175730", "N0000175737"], "upc": ["0315014910109"], "unii": ["125OD7737X"], "rxcui": ["197943"], "spl_set_id": ["35c044a6-90c0-55f8-e063-6294a90aad48"], "pharm_class_pe": ["Centrally-mediated Muscle Relaxation [PE]"], "pharm_class_epc": ["Muscle Relaxant [EPC]"], "manufacturer_name": ["GENTEX PHARMA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (15014-910-10)", "package_ndc": "15014-910-10", "marketing_start_date": "20250522"}], "brand_name": "Methocarbamol", "product_id": "15014-910_35c044a6-90c1-55f8-e063-6294a90aad48", "dosage_form": "TABLET", "pharm_class": ["Centrally-mediated Muscle Relaxation [PE]", "Muscle Relaxant [EPC]"], "product_ndc": "15014-910", "generic_name": "methocarbamol", "labeler_name": "GENTEX PHARMA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methocarbamol", "active_ingredients": [{"name": "METHOCARBAMOL", "strength": "500 mg/1"}], "application_number": "ANDA040489", "marketing_category": "ANDA", "marketing_start_date": "20250522", "listing_expiration_date": "20261231"}